for our pharmaceutical manufacturing facility engaged in
tablets, capsules, and external preparations
. The ideal candidate must possess
State FDA Approval (Competent Person)
for
minimum approval in tablet and capsule manufacturing
and demonstrate a deep understanding of
WHO-GMP guidelines
and
Schedule M compliance
.
Key Responsibilities:
Oversee and manage daily production operations for
tablets, capsules, and external preparations
.
Ensure strict compliance with
WHO-GMP
,
Revised Schedule M
, and internal SOPs.
Maintain documentation and batch records as per cGMP requirements.
Plan and implement production schedules to meet delivery timelines.
Supervise, train, and manage production staff for optimal performance and quality.
Monitor equipment maintenance and ensure smooth functioning of all machinery.
Coordinate with QA/QC departments to resolve deviations, non-conformities, or quality issues.
Maintain cleanroom and environmental control protocols.
Ensure optimal utilization of raw materials, manpower, and machines.
Participate actively in audits (regulatory/internal) and ensure compliance.
Candidate Requirements:
Education
:
B.Pharm / B.Sc. / M.Sc. in relevant field (Postgraduate qualification preferred)
Approvals
State FDA Approval
Competent Person
minimum approval in tablet and capsule manufacturing
Experience
:
15-20 years of relevant experience in pharmaceutical production (solid dosage and external formulations).
Skills
:
Sound knowledge of GMP and manufacturing processes
Strong leadership and team management skills
Good communication and problem-solving abilities
Familiarity with regulatory audits and documentation
Perks & Benefits:
Competitive salary
Professional growth opportunities
Work in a reputed pharma company with GMP-certified facility
Share Resume on our Official WhatsApp's number :-
9541420147
Mail ID :-
recruiter.vpj@gmail.com
Job Type: Full-time
Pay: ₹1,200,000.00 - ₹1,400,000.00 per year
Schedule:
Day shift
Work Location: In person
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